Regulatory and Start Up Specialist 2

**Job Overview** Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. **_At least 3 years' experience with submissions....

We are looking for an experienced regulatory ecotoxicologist to work as a technical specialist in a multi-disciplinary registrations team. The role will involve acting as the department ecotox expert, you will mentor more junior ecotoxicologists and provide expert advice and guidance to external stakeholders. The role will involve supporting large...

We’re looking for a ** Site Start Up Associate II **to join our ** Study Start Up** team that is passionate about improving healthcare through innovative clinical research. As a member of the Premier Research team, you’ll help create tangible solutions for patients in need while building cross-functional partnerships that enable your growth and...

**Accounts Receivable Specialist - Part-Time (approx 1 day per week)** **Why Work for GrantUp?** At GrantUp, we are committed to helping innovative projects secure vital funding through expert grant consultancy services. With a proven track record of over £60 million in raised funds, our team is dedicated to driving success. Join us to be part of a...

REF: - INTERCONNECTEMEA00285- DIVISION: - Smiths Interconnect- JOB FUNCTION: - Legal and ComplianceAbout us - Employing over 2,000 people globally our in house capabilities encompass design, development, manufacturing and testing to respond quickly and accurately to customer's needs and provide the most reliable connectivity solutions.We have a fantastic...

Sr Country Approval Specialist (Study Start-up / Submissions Specialist) At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to...

Parexel FSP has an exciting opportunity for a Vendor Start-up Manager to join our single sponsor dedicated team, based in either the UK or Ireland.Job Summary:The Vendor Start-up Manager (VSM) will provide technical expertise for the category throughout start-up to close out to the VCE (Vendor Category Expert) and indirectly to the Clinical Trial Team.The...

Parexel FSP has an exciting opportunity for a Vendor Start-up Manager to join our single sponsor dedicated team, based in either the UK or Ireland.Job Summary:The Vendor Start-up Manager (VSM) will provide technical expertise for the category throughout start-up to close out to the VCE (Vendor Category Expert) and indirectly to the Clinical Trial Team.The...

Sr Country Approval Specialist (Study Start-up / Submissions Specialist) At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to...

DescriptionSenior Site Activation SpecialistSyneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our...

We are currently looking for Regulatory Affairs Professionals experienced in Clinical Trail Applications (CTAs) under EU-CTR directive. You can join us or our client dedicated projects and act as a Regulatory Affairs Consultant or Regulatory Affairs Senior Associate. This role can be based in either UK or UE (home/office based). In this role you will provide...

We are currently looking for Regulatory Affairs Professionals experienced in Clinical Trail Applications (CTAs) under EU-CTR directive. You can join us or our client dedicated projects and act as a Regulatory Affairs Consultant or Regulatory Affairs Senior Associate. This role can be based in either UK or UE (home/office based). In this role you will provide...

**Description** **Senior Site Activation Specialist** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to...

We are looking for a Senior Medical Regulatory Writer for our global health communications client that has offices based in Manchester but with fully remote working available. Our client partners work with global pharmaceutical and biotechnology companies to provide expertise in strategic consultancy, multi-channel medical communications and regulatory...

Discipline: - Retail Banking- Job type: - Permanent- Contact name: - Hannah Eustace- Job ref: - 020483- Published: - 3 minutes ago**Payments Specialist (Change)** **Salary up to £48,300** **Grade: CR3** **Location: Home Based** **Hours: 35 per week** **Job purpose**: We are excited to announce a brand new opportunity for a Payments Specialist to work...

The purpose of the Global Labelling group is to drive the core labelling strategy and ensure that labelling documents are of high quality and compliant for the safe and effective use of our products for patients and healthcare providers globally. As the Global Labelling Lead, you would be responsible for developing the strategy and leading the development...

The purpose of the Global Labelling group is to drive the core labelling strategy and ensure that labelling documents are of high quality and compliant for the safe and effective use of our products for patients and healthcare providers globally. As the Global Labelling Lead, you would be responsible for developing the strategy and leading the development...

EXCITING SMALL BUSINESS OPPORTUNITY! ACT ALCOHOL DEPENDENCY SPECIALIST - ASSOCIATE TEAM MEMBER We are looking to train new ACT associate team members around the UK. - This business and training opportunity requires an investment of £3225 to become an ACT Certified Practitioner * Who can apply? Qualified & Student Counsellors, Psychotherapists, Social...

Parexel FSP is currently looking for an experienced Regulatory & Submissions Lead to join our expanding team in the UK.This will be a home-based position.Working at Parexel offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. We have an incredible...

Overview: Regulatory Writers provide support on the development of high quality documentation for regulatory submissions in order to help streamline the regulatory documentation process for our clients. The Regulatory Writer I (RW I) will support senior writers in the creation of a variety of documents across different service lines. The RW I will provide...